Senior Clinical Research Coordinator - Multi-Site Trials

Equity Medical LLC.; Nashville (TN); On-site; USD 60,000 - 80,000; Full time

Job summary

Equity Medical LLC. is seeking an experienced Clinical Research Coordinator for our Nashville, Tennessee site. We conduct Phase I-IV trials across dermatology, allergy/immunology, respiratory, rheumatology, neurology and metabolic diseases.

The role requires 3+ years of coordination experience, knowledge of interventional trials, and a strong grasp of GCP and FDA regulations. You will manage multiple studies, interact with sponsors and CROs, and oversee day-to-day site operations.

Qualifications

• Bachelor's degree or equivalent required.
• 3+ years clinical research coordination experience preferred.
• Interventional pharmaceutical-sponsored trials experience required.
• Strong knowledge of GCP and FDA regulations.
• Experience managing multiple studies independently.

Responsibilities

• Coordinate all aspects of assigned trials from startup through closeout.
• Independently manage visits, scheduling, source docs, and data entry.
• Ensure protocol compliance, GCP and regulatory adherence.
• Recruit, screen, and consent participants.
• Communicate with sponsors, CROs, monitors, investigators, and participants.
• Maintain audit-ready regulatory and study documentation.
• Support monitoring visits and sponsor communications.
• Assist with startup activities and regulatory submissions.

Skills

Interventional trials experience

Study coordination

Regulatory compliance

Data entry / source documentation

Communication skills

Organizational skills

Education

Bachelor's degree or equivalent

Job description

Equity Medical LLC. is seeking an experienced Clinical Research Coordinator for our Nashville, Tennessee site. We conduct Phase I-IV trials across dermatology, allergy/immunology, respiratory, rheumatology, neurology and metabolic diseases.

The role requires 3+ years of coordination experience, knowledge of interventional trials, and a strong grasp of GCP and FDA regulations. You will manage multiple studies, interact with sponsors and CROs, and oversee day-to-day site operations.